Canonical Allele Identifier: PA2580462401
Gene: CEP97 HGNC NCBI

Linked Data

ClinVar Variation Id: 2198695
ClinVar RCV Id: RCV002633809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078824.2:p.Asp496Val
CA2522137
NM_024548.4:c.1487A>T